"Quest Diagnostics Nichols Institute San Juan Capistrano"[submitter] A - ClinVar

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Search results

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2685986	GRCh37/hg19 4q26-32.3(chr4:117518683-168174703)x3	SPOCK3, SPRY1 +153 more	Copy number gain	not provided	GPathogenic
Select item 1809215	GRCh37/hg19 4q32.2(chr4:162443332-163119356)x3	FSTL5	Copy number gain	not provided	GUncertain significance
Select item 1808848	GRCh37/hg19 4q32.2(chr4:162134811-162505383)x1	FSTL5	Copy number loss	not provided	GUncertain significance
Select item 1808190	GRCh37/hg19 4q32.1-32.3(chr4:161461677-166911259)x1	ANP32C, CPE +14 more	Copy number loss	not provided	GUncertain significance
Select item 980705	GRCh37/hg19 4q32.1-32.2(chr4:161257840-162828600)x3	FSTL5	Copy number gain	not provided	GUncertain significance
Select item 814619	GRCh37/hg19 4q32.2(chr4:162967232-163493491)x3	FSTL5	Copy number gain	not provided	GLikely benign
Select item 562992	GRCh37/hg19 4q32.2(chr4:162698219-163047747)x1	FSTL5	Copy number loss	not provided	GUncertain significance
Select item 562991	GRCh37/hg19 4q32.2(chr4:162519814-163118339)x1	FSTL5	Copy number loss	not provided	GUncertain significance
Select item 562990	GRCh37/hg19 4q32.2(chr4:161937082-162744835)x1	FSTL5	Copy number loss	not provided	GLikely benign
Select item 562989	GRCh37/hg19 4q32.1-35.2(chr4:159492464-190957473)x3	AADAT, ACSL1 +92 more	Copy number gain	not provided	GPathogenic
Select item 562986	GRCh37/hg19 4q32.1-35.1(chr4:157552397-183831253)x3	AADAT, ADAM29 +60 more	Copy number gain	not provided	GPathogenic